Process Development Associate (1st Shift)

SGS_JOB_1333

Industrial
 California
Process Development
Manufacturing Processes
GMP Compliance
Process Validation
Laboratory Operations

Contract - 6 Months + (Possibility of Extension)

Hours: 6:30am - 3:00pm (Monday to Friday) We are looking for a Process Development Associate to join our team. In this role, you will support the creation and transfer of manufacturing processes from R&D to manufacturing while ensuring compliance with Good Manufacturing Practices (GMP). The ideal candidate will have a solid understanding of manufacturing processes and laboratory operations, with experience in process development and process validation.

Job Responsibilities:

  • Assist in the creation, development, and transfer of manufacturing processes from R&;D to manufacturing.
  • Maintain and operate the Pilot Plant laboratory in compliance with cGMP (current Good Manufacturing Practices) standards.
  • Produce development, pilot, and production materials per written instructions.
  • Complete ERP transactions and maintain accurate inventory of laboratory supplies.
  • Ensure all records and documentation are completed on time and accurately.
  • Assist in the execution of process validation for new and existing manufacturing processes.
  • Support continuous improvement initiatives to optimize manufacturing processes.
  • Complete cycle counts and maintain proper inventory control.
  • Ensure safety standards are met, including the safe handling of hazardous materials and chemicals.
  • Maintain cleanliness and organization of the laboratory and workspace.
  • Follow written procedures to complete laboratory tasks and associate paperwork.

Skills:

  • Knowledge of cGMP and manufacturing processes.
  • Familiarity with process development and validation.
  • Ability to work with laboratory equipment and maintain accurate records.
  • Strong problem-solving skills and attention to detail.
  • Ability to lift and carry up to 40 lbs and perform tasks that may involve standing, bending, or walking.
  • Comfortable working in an environment with potential exposure to hazardous chemicals or materials.
  • Ability to follow written procedures and work within safety and quality standards.

Education/Experience:

  • Bachelor’s degree in a scientific field (e.g., Biology, Chemistry, or related discipline).
  • 1+ years of experience in a manufacturing or laboratory environment preferred.
  • Familiarity with QMS (Quality Management System) and GMP regulations.
  • Ability to work well independently and as part of a team.
  • Excellent organizational skills and the ability to prioritize tasks.

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